• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

靶向肠道 TMPRSS2 蛋白酶以阻止 SARS-CoV-2 进入肠上皮细胞——前景与挑战。

Targeting the intestinal TMPRSS2 protease to prevent SARS-CoV-2 entry into enterocytes-prospects and challenges.

机构信息

Department of Medical Laboratory Sciences, Faculty of Allied Health Sciences, The Hashemite University, Zarqa, 13133, Jordan.

Department of Pharmacy, Alzaytoonah University of Jordan, Amman, Jordan.

出版信息

Mol Biol Rep. 2021 May;48(5):4667-4675. doi: 10.1007/s11033-021-06390-1. Epub 2021 May 22.

DOI:10.1007/s11033-021-06390-1
PMID:34023987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8140747/
Abstract

The transmembrane protease serine 2 (TMPRSS2) is a membrane anchored protease that primarily expressed by epithelial cells of respiratory and gastrointestinal systems and has been linked to multiple pathological processes in humans including tumor growth, metastasis and viral infections. Recent studies have shown that TMPRSS2 expressed on cell surface of host cells could play a crucial role in activation of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein which facilitates the rapid early entry of the virus into host cells. In addition, direct suppression of TMPRSS2 using small drug inhibitors has been demonstrated to be effective in decreasing SARS-CoV-2 infection in vitro, which presents TMPRSS2 protease as a potential therapeutic strategy for SARS-CoV-2 infection. Recently, SARS-CoV-2 has been shown to be capable of infecting gastrointestinal enterocytes and to provoke gastrointestinal disorders in patients with COVID-19 disease, which is considered as a new transmission route and target organ of SARS-CoV-2. In this review, we highlight the biochemical properties of TMPRSS2 protease and discuss the potential targeting of TMPRSS2 by inhibitors to prevent the SARS-CoV-2 spreading through gastro-intestinal tract system as well as the hurdles that need to be overcome.

摘要

跨膜丝氨酸蛋白酶 2(TMPRSS2)是一种膜锚定蛋白酶,主要表达于呼吸系统和消化系统的上皮细胞,与人类的多种病理过程有关,包括肿瘤生长、转移和病毒感染。最近的研究表明,宿主细胞表面表达的 TMPRSS2 在严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突蛋白的激活中起着至关重要的作用,这有助于病毒快速早期进入宿主细胞。此外,使用小分子药物抑制剂直接抑制 TMPRSS2 已被证明可有效减少 SARS-CoV-2 在体外的感染,这表明 TMPRSS2 蛋白酶是 SARS-CoV-2 感染的潜在治疗策略。最近的研究表明,SARS-CoV-2 能够感染胃肠道肠细胞,并在 COVID-19 患者中引发胃肠道疾病,这被认为是 SARS-CoV-2 的新传播途径和靶器官。在这篇综述中,我们强调了 TMPRSS2 蛋白酶的生化特性,并讨论了抑制剂靶向 TMPRSS2 以阻止 SARS-CoV-2 通过胃肠道系统传播的潜力,以及需要克服的障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0d0/8140747/6b85148264da/11033_2021_6390_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0d0/8140747/ba4e568fde53/11033_2021_6390_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0d0/8140747/6b85148264da/11033_2021_6390_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0d0/8140747/ba4e568fde53/11033_2021_6390_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0d0/8140747/6b85148264da/11033_2021_6390_Fig2_HTML.jpg

相似文献

1
Targeting the intestinal TMPRSS2 protease to prevent SARS-CoV-2 entry into enterocytes-prospects and challenges.靶向肠道 TMPRSS2 蛋白酶以阻止 SARS-CoV-2 进入肠上皮细胞——前景与挑战。
Mol Biol Rep. 2021 May;48(5):4667-4675. doi: 10.1007/s11033-021-06390-1. Epub 2021 May 22.
2
The TMPRSS2 Inhibitor Nafamostat Reduces SARS-CoV-2 Pulmonary Infection in Mouse Models of COVID-19.TMPRSS2 抑制剂那法莫司他可降低 COVID-19 小鼠模型中的 SARS-CoV-2 肺部感染。
mBio. 2021 Aug 31;12(4):e0097021. doi: 10.1128/mBio.00970-21. Epub 2021 Aug 3.
3
Structural Basis of Covalent Inhibitory Mechanism of TMPRSS2-Related Serine Proteases by Camostat.抑肽酶对TMPRSS2相关丝氨酸蛋白酶共价抑制机制的结构基础
J Virol. 2021 Sep 9;95(19):e0086121. doi: 10.1128/JVI.00861-21. Epub 2021 Jun 23.
4
Alpha-1 antitrypsin inhibits TMPRSS2 protease activity and SARS-CoV-2 infection.α-1 抗胰蛋白酶抑制 TMPRSS2 蛋白酶活性和 SARS-CoV-2 感染。
Nat Commun. 2021 Mar 19;12(1):1726. doi: 10.1038/s41467-021-21972-0.
5
The Transmembrane Protease TMPRSS2 as a Therapeutic Target for COVID-19 Treatment.跨膜蛋白酶 TMPRSS2 作为 COVID-19 治疗的治疗靶点。
Int J Mol Sci. 2022 Jan 25;23(3):1351. doi: 10.3390/ijms23031351.
6
Synergistic Block of SARS-CoV-2 Infection by Combined Drug Inhibition of the Host Entry Factors PIKfyve Kinase and TMPRSS2 Protease.联合抑制宿主进入因子 PIKfyve 激酶和 TMPRSS2 蛋白酶对 SARS-CoV-2 感染的协同阻断。
J Virol. 2021 Oct 13;95(21):e0097521. doi: 10.1128/JVI.00975-21. Epub 2021 Aug 18.
7
Targeting the viral-entry facilitators of SARS-CoV-2 as a therapeutic strategy in COVID-19.针对 SARS-CoV-2 的病毒进入促进剂作为 COVID-19 的治疗策略。
J Med Virol. 2021 Sep;93(9):5260-5276. doi: 10.1002/jmv.27019. Epub 2021 May 3.
8
Spiking dependence of SARS-CoV-2 pathogenicity on TMPRSS2.刺突依赖性 SARS-CoV-2 致病性与 TMPRSS2 相关。
J Med Virol. 2021 Jul;93(7):4205-4218. doi: 10.1002/jmv.26911. Epub 2021 Mar 18.
9
Topical TMPRSS2 inhibition prevents SARS-CoV-2 infection in differentiated human airway cultures.局部抑制 TMPRSS2 可预防人呼吸道分化细胞中 SARS-CoV-2 的感染。
Life Sci Alliance. 2022 Feb 2;5(4). doi: 10.26508/lsa.202101116. Print 2022 Apr.
10
The Transmembrane Protease Serine 2 (TMPRSS2) Non-Protease Domains Regulating Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Spike-Mediated Virus Entry.跨膜丝氨酸蛋白酶 2(TMPRSS2)非蛋白酶结构域调节严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)刺突介导的病毒进入。
Viruses. 2023 Oct 19;15(10):2124. doi: 10.3390/v15102124.

引用本文的文献

1
The S2 Glycoprotein Subunit Determines Intestinal Tropism in Infectious Bronchitis Virus.S2糖蛋白亚基决定传染性支气管炎病毒的肠道嗜性。
Microorganisms. 2025 Aug 17;13(8):1918. doi: 10.3390/microorganisms13081918.
2
Bacterial Proteases as Potentially Exploitable Modulators of SARS-CoV-2 Infection: Logic from the Literature, Informatics, and Inspiration from the Dog.细菌蛋白酶作为新冠病毒感染潜在可利用的调节剂:来自文献的逻辑、信息学以及犬类的启示
BioTech (Basel). 2023 Oct 30;12(4):61. doi: 10.3390/biotech12040061.
3
A Tale of Two Proteases: M and TMPRSS2 as Targets for COVID-19 Therapies.

本文引用的文献

1
Relevance of SARS-CoV-2 related factors ACE2 and TMPRSS2 expressions in gastrointestinal tissue with pathogenesis of digestive symptoms, diabetes-associated mortality, and disease recurrence in COVID-19 patients.SARS-CoV-2 相关因素 ACE2 和 TMPRSS2 在胃肠道组织中的表达与 COVID-19 患者发病机制中的消化道症状、糖尿病相关死亡率和疾病复发的相关性。
Med Hypotheses. 2020 Nov;144:110271. doi: 10.1016/j.mehy.2020.110271. Epub 2020 Sep 13.
2
Expression and co-expression analyses of TMPRSS2, a key element in COVID-19.TMPRSS2 的表达和共表达分析,COVID-19 的关键因素。
Eur J Clin Microbiol Infect Dis. 2021 Feb;40(2):451-455. doi: 10.1007/s10096-020-04089-y. Epub 2020 Nov 27.
3
两种蛋白酶的故事:M和跨膜丝氨酸蛋白酶2作为新冠病毒疗法的靶点
Pharmaceuticals (Basel). 2023 Jun 2;16(6):834. doi: 10.3390/ph16060834.
4
Modulation of IRAK enzymes as a therapeutic strategy against SARS-CoV-2 induced cytokine storm.作为一种治疗策略,针对 SARS-CoV-2 诱导的细胞因子风暴对 IRAK 酶进行调节。
Clin Exp Med. 2023 Oct;23(6):2909-2923. doi: 10.1007/s10238-023-01064-7. Epub 2023 Apr 15.
5
Targeting Human Proteins for Antiviral Drug Discovery and Repurposing Efforts: A Focus on Protein Kinases.靶向人类蛋白的抗病毒药物发现和再利用研究:以蛋白激酶为重点。
Viruses. 2023 Feb 19;15(2):568. doi: 10.3390/v15020568.
6
Multi-Omic Factors Associated with Frequency of Upper Respiratory Infections in Developing Infants.与发展中婴儿上呼吸道感染频率相关的多组学因素。
Int J Mol Sci. 2023 Jan 4;24(2):934. doi: 10.3390/ijms24020934.
7
Impact of Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2.表达、突变预后以及小分子(CD、AD、TQ 和 TQFL12)抑制对泛癌肿瘤的影响和对 SARS-CoV-2 的易感性。
Molecules. 2022 Nov 1;27(21):7413. doi: 10.3390/molecules27217413.
8
Increased TRIM31 gene expression is positively correlated with SARS-CoV-2 associated genes TMPRSS2 and TMPRSS4 in gastrointestinal cancers.TRIM31 基因表达的增加与胃肠道癌症中 SARS-CoV-2 相关基因 TMPRSS2 和 TMPRSS4 呈正相关。
Sci Rep. 2022 Aug 15;12(1):11763. doi: 10.1038/s41598-022-15911-2.
9
Factors Modulating COVID-19: A Mechanistic Understanding Based on the Adverse Outcome Pathway Framework.调节2019冠状病毒病的因素:基于不良结局途径框架的机制理解
J Clin Med. 2022 Jul 31;11(15):4464. doi: 10.3390/jcm11154464.
10
Multifaceted roles of plant derived small molecule inhibitors on replication cycle of SARS-CoV-2.植物源小分子抑制剂对 SARS-CoV-2 复制周期的多方面作用。
Microb Pathog. 2022 Jul;168:105512. doi: 10.1016/j.micpath.2022.105512. Epub 2022 Apr 2.
Aprotinin Inhibits SARS-CoV-2 Replication.
抑肽酶抑制 SARS-CoV-2 复制。
Cells. 2020 Oct 30;9(11):2377. doi: 10.3390/cells9112377.
4
ACE2/ADAM17/TMPRSS2 Interplay May Be the Main Risk Factor for COVID-19.ACE2/ADAM17/TMPRSS2 相互作用可能是 COVID-19 的主要风险因素。
Front Immunol. 2020 Oct 7;11:576745. doi: 10.3389/fimmu.2020.576745. eCollection 2020.
5
Coronaviruses and gastrointestinal diseases.冠状病毒与胃肠道疾病。
Mil Med Res. 2020 Oct 14;7(1):49. doi: 10.1186/s40779-020-00279-z.
6
Effect of bromhexine on clinical outcomes and mortality in COVID-19 patients: A randomized clinical trial.氨溴索对新型冠状病毒肺炎患者临床结局及死亡率的影响:一项随机临床试验。
Bioimpacts. 2020;10(4):209-215. doi: 10.34172/bi.2020.27. Epub 2020 Jul 19.
7
Robust and persistent SARS-CoV-2 infection in the human intestinal brush border expressing cells.在表达人肠道刷状缘的细胞中存在稳健且持久的 SARS-CoV-2 感染。
Emerg Microbes Infect. 2020 Dec;9(1):2169-2179. doi: 10.1080/22221751.2020.1827985.
8
Gene of the month: (transmembrane serine protease 2).本月基因:(跨膜丝氨酸蛋白酶2)。
J Clin Pathol. 2020 Dec;73(12):773-776. doi: 10.1136/jclinpath-2020-206987. Epub 2020 Sep 1.
9
Expression profiling meta-analysis of ACE2 and TMPRSS2, the putative anti-inflammatory receptor and priming protease of SARS-CoV-2 in human cells, and identification of putative modulators.ACE2 和 TMPRSS2 的表达谱荟萃分析,SARS-CoV-2 在人细胞中的假定抗炎受体和启动蛋白酶,以及假定调节剂的鉴定。
Redox Biol. 2020 Sep;36:101615. doi: 10.1016/j.redox.2020.101615. Epub 2020 Jun 24.
10
Coronavirus: Why Men are More Vulnerable to Covid-19 Than Women?冠状病毒:为何男性比女性更容易感染新冠病毒?
SN Compr Clin Med. 2020;2(7):874-876. doi: 10.1007/s42399-020-00341-w. Epub 2020 Jun 4.